The Senior Statistical Programmer will oversee the verification of datasets formatted to submission-ready standards (Adam), along with tables, figures, listings, and submission packages. They will offer specialized guidance in the design, execution, and quality assurance of SAS programs, enabling the extraction, transformation, review, analysis, and submission of clinical data for all required analyses.
Why Join IQVIA?
Partner with key stakeholders in the industry to spearhead projects that drive clinical innovation forward.
Acquire experience across diverse therapeutic domains, indications, and clinical development phases to broaden your expertise and enhance professional growth.
We offer robust career development initiatives designed to support your professional growth alongside our organization’s expansion. Our internal talent marketplace leverages AI to streamline and enhance career advancement opportunities. Additionally, we facilitate Career Connections to foster meaningful professional relationships and further your career journey.
Employees can engage in mentorship opportunities throughout the organization through Employee Resource Groups.
Flexible working arrangements are provided to support both a healthy work–life balance and ongoing professional development.
Join an organization recognized as a 2026 Fortune World’s Most Admired Company—a prestigious distinction achieved for the fifth consecutive year.
Oversee daily operations to ensure efficiency and adherence to established protocols, prioritizing tasks to meet organizational objectives. Collaborate with cross-functional teams to align projects with strategic goals and foster innovation. Develop and implement policies, procedures, and performance metrics to enhance productivity and accountability. Monitor key performance indicators to identify trends, address inefficiencies, and drive continuous improvement. Serve as a liaison between senior management and staff, facilitating clear communication and resolving escalated issues. Ensure compliance with industry regulations, safety standards, and ethical guidelines while maintaining a high standard of operational excellence.
Works alongside study teams to develop data architecture and detailed specifications for various ad hoc and study deliverables, such as Adam datasets, tables, figures, listings, and analysis submission content.
Works collaboratively with study teams to validate the integrity and correctness of clinical data, ensuring it meets submission standards set by regulatory bodies (such as SDTM, Adam, tables, figures, listings, and define.xml) and is prepared for timely submission.
Leads and manages pooled and exploratory analyses, collaborating closely with the Statistics TA lead and/or study statisticians, as well as the clinical programming team and their legacy data collection efforts.
Leads and manages the internal development and execution of ISS and IS datasets, along with related deliverables such as tables, figures, and listings, in instances where these are not furnished by the Contract Research Organization (CRO).
Our team seeks a skilled professional to spearhead the design and execution of sophisticated SAS programs, specifically tailored for applications that analyze and report intricate clinical trial data in DISC Adam format. The role involves leading comprehensive projects from inception through implementation, ensuring alignment with regulatory standards and data integrity requirements. Responsibilities include developing robust SAS solutions, collaborating with cross-functional teams, and maintaining meticulous documentation to support accurate data interpretation and decision-making.
Directs and manages the creation of comprehensive, worldwide resources designed to enhance both the effectiveness and of the Statistical Programming division.
Collaborates closely with clinical study teams to strategize and implement activities, ensuring adherence to project timelines while maintaining superior quality standards in all deliverables.
Works collaboratively with CR&D staff to address data analysis requests, ensuring alignment with project objectives and accuracy in findings.
Conducts supplementary statistical evaluations encompassing, but not limited to, the following tasks:
Prepare regulatory agency responses by providing comprehensive support, ensuring all submissions adhere to applicable guidelines and timelines.
Compile comprehensive summaries that encompass both safety and efficacy data to provide a cohesive overview of clinical trial outcomes.
Assist in the development and dissemination of publications and presentations to ensure effective communication of key information.
Facilitate the planning and reporting of clinical trials by conducting in-depth exploratory analyses of existing data.
The position necessitates a minimum of five years of relevant professional experience, along with a bachelor’s degree in a related field. Proficiency in industry-standard software and tools is essential, alongside strong analytical and problem-solving abilities. Candidates must demonstrate excellent communication skills, both written and verbal, to effectively collaborate with cross-functional teams. Additionally, the role requires the capacity to manage multiple priorities in a fast-paced environment while maintaining a high level of attention to detail. A proven track record of delivering successful projects within specified timelines is also expected.
A relevant degree in Computer Science, Mathematics, Statistics, or a closely related field, supported by applicable professional experience, is required.
With a minimum of five years of hands-on experience in clinical programming and/or statistical programming within the contract research organization or pharmaceutical industry, leveraging SAS Software, you will bring a strong technical foundation to the role.
Demonstrates a comprehensive grasp of clinical programming methodologies and statistical programming principles, along with their associated processes and industry standards.
Professional candidates will demonstrate substantial expertise in statistical programming, with a focus on SAS software, including the development and implementation of SAS Macros. Additionally, they should possess robust programming capabilities and exceptional problem-solving aptitude.
Acquired practical expertise through hands-on implementation of R Programming.
Proficiency in DISC standards, including CASH, SDTM, and Adam, is essential.
Accomplished professionals must demonstrate a strong background in directing programming initiatives for pooled and exploratory analyses spanning various clinical studies, as well as submission-related activities.
Demonstrates the capacity to thrive in both independent and collaborative environments while consistently achieving established objectives through self-directed timeline management.
Skilled in collaborating within diverse, multicultural, and international clinical trial teams that operate across multiple functions, with proven adaptability to varied work environments and team dynamics.
Qualifications
BA/BSc/HND
Experience Required
5 years
